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Combine effect of tab melatonin and pectointercostal fascial block on postoperative pain management in patients undergoing open heart surgeries.

To study the effect of combination, oral melatonin and pectointercostal fascial block for postoperative pain management in patients undergoing open cardiac surgery- Prospective randomized study. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067707
Enrollment
40
Registered
2024-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Tab melatonin 5 mg: Tab melatonin 5 mg will be given to 120 min before surgery in intervention group. Postoperative pain scores upto 24 hrs, will be monitored. Control Intervention1: ta

Sponsors

AIIMS Raipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Adult patients aged 18-to-80 years -ASA grades II- to-III -Patients scheduled for elective on-pump cardiac surgery requiring median sternotomies such as coronary artery bypass grafting (CABG), CABG with or without valve replacement, and isolated valve surgeries will include in the study.

Exclusion criteria

Exclusion criteria: -emergency surgery, -an allergy to local anaesthetics, -hemodynamic instability (left ventricular ejection fraction & EF 30%) -congestive heart failure, hepatic or renal failure, -a history of drug abuse or chronic pain, -psychiatric problems, -secondary surgery, - inability to provide inform

Design outcomes

Primary

MeasureTime frame
To assess whether the combination of melatonin and B/L pectointercostal fascial block provides prolonged adequate analgesia and promotes rapid recovery.Timepoint: numeric rating scale (NRS) at 0, 3, 6-, 12-, 18-, and 24-hours during breathing of normal tidal volume and with cough.

Secondary

MeasureTime frame
The requirement of fentanyl during the postoperative period, extubation time, postoperative delirium and length of ICU, and hospital stay. To evaluate anxiety and sedation levels in the preoperative area before shifting to the 9 operation theatre.Timepoint: preoperative, postoperatively 24 hrs

Countries

India

Contacts

Public ContactDrJitendra kalbande

aiims raipur

drjitu222@gmail.com08368326094

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026